Interactome Analysis of 11-Dehydrosinulariolide-Treated Oral Carcinoma Cell Lines Such as Ca9-22 and CAL-27 and Melanoma Cell Line

Article Type:
Research/Original Article (دارای رتبه معتبر)
Abstract:
Background
Oral squamous cell carcinoma (OSCC) is one of the most common malignancies in head and neck. The patients usually have a poor prognosis because they do not understand the significance of early symptoms. Then, the timely treatment may be lost. In recent years, network analysis is growing in the target identification concepts and can provide opportunities in pathway analysis. These could provide valuable information for drug development and progression monitoring of cancers such as OSCC.
Methods
PubMed Database was used as the main source and “Oral cancer” and “11-dehydrosinulariolide” and “Proteomics” were the keywords for the search process. We focused on articles that studied the differentially expressed proteins of cell lines of OSCC (Ca9-22 and CAL-27) and melanoma cell line (A2058) after 11-dehydrosinulariolideon treatment. The topological features of differentially expressed proteins were analyzed using Cytoscape Version 3.4.0. Module selection of the protein-protein interactions (PPI) networks was done using MCODE plug-in. In addition, gene ontology (GO) enrichment analysis of modules in related PPI networks was assessed.
Results
Network analysis show that UBC, HSPA5 and GAPDH are the common central proteins between the three treated cell lines. The GO terms of the gene list of each of the correlated modules of networks are mostly related to four functions such as protein folding and assembly, metabolic processes, translation, and apoptotic pathways.
Conclusions
Despite introduction of different protein panels related to the effect of 11-dehydrosinulariolide on cancerous cell lines in the previous studies, here a common biomarker panel is represented.
Language:
English
Published:
International Journal of Cancer Management, Volume:10 Issue: 7, Jul 2017
Page:
2
magiran.com/p1774393  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!